CLINICAL TRIALS TECHNICIAN

NEBRASKA HEMATOLOGY ONCOLOGY (NHO); Lincoln (NE); On-site; USD 42,000 - 65,000; Full time

Job summary

Nebraska Hematology-Oncology, PC in Lincoln, NE seeks a Clinical Trial Technician to coordinate and perform patient-specific procedures across multiple studies, including phlebotomy, specimen processing, electrocardiograms, and vital signs, in strict accordance with SOPs and study protocols.

Requirements include at least 1 year of phlebotomy experience; clinical research exposure with lab sample handling and EKGs is preferred.

Qualifications

• At least 1 year of phlebotomy experience.
• Clinical research experience with sample collection/processing preferred.
• Experience with EKGs and vital signs preferred.

Responsibilities

• Perform clinical trial procedures for studies led by principal investigators at Nebraska Hematology-Oncology, PC.
• Participate in study initiation visits, source document creation/review, and cross-department planning (lab and sample collection).
• Confirm study visit lab orders are accurate in preparation for visits.
• Ensure billing compliance for study-related lab testing.
• Perform lab collection including phlebotomy, processing, storage, packaging, and shipment across multiple studies.
• Collect vital signs and perform electrocardiograms in collaboration with clinical trials coordinators.
• Assess patient-reported outcomes/diary compliance with coordinators.
• Ensure compliance with SOPs, FDA, and regulatory agencies; perform related duties.
• Perform phlebotomy as needed for routine patient care.

Skills

Detail orientation

Communication skills

Medical terminology

Safety awareness

Record keeping

Interpersonal skills

Problem solving

Job description

Description

JOB TITLE:

Clinical Trial Technician

JOB SUMMARY:

Coordinate and participate in clinical research studies conducted by principal investigators at Nebraska Hematology-Oncology, PC, performing clinical trial patient specific procedures including phlebotomy, specimen processing, electrocardiograms, and vital signs across multiple studies in accordance to appropriate regulations, Standard Operating Procedures, and study specific protocols/manuals.

TYPICAL PHYSICAL DEMANDS:

Requires full range of motion including manual and finger dexterity and eye-hand coordination. Frequent standing and walking required for extended periods of time. Lifts and carries items weighing up to 50 pounds. Requires visual acuity and normal color perception.

REPORTS TO:

Clinical Trials Manager

EDUCATION/EXPERIENCE:

At least 1 year of experience as a phlebotomist. Clinical research experience in the collection and processing of lab samples, EKGs, vital signs preferred.

DUTIES/RESPONSIBILITIES:

• Perform clinical trial procedures for clinical research studies conducted by principal investigator(s) at Nebraska Hematology-Oncology, PC.
• Participate in study initiation visits, source document creation/review, planning for cross-departmental procedures (such as with laboratory and sample collection from vascular access devices)
• Confirm study visit lab orders are accurate in preparation for visit
• Ensure billing compliance for study-related lab testing
• Perform study lab collection including phlebotomy, lab sample processing, storage, packaging and shipment across multiple studies simultaneously
• Perform vital signs collection and electrocardiograms in collaboration with clinical trials coordinators
• Assess/facilitate study-specific patient reported outcomes/diary compliance in collaboration with clinical trials coordinators
• Assure compliance of general and study specific processes with SOPs, the FDA, and applicable regulatory agencies.
• Perform other related duties incidental to the work described herein.
• Perform phlebotomy if/as needed for routine patient care

Requirements

REQUIRED SKILLS/ABILITIES:

• Applicant should be detail-oriented with excellent communication skills.
• Position will require interaction with patients, study sponsors, the research team, and principal investigators.
• Knowledge of organizational policies, regulations, and procedures to administer clinical research protocols.
• Knowledge of medical terminology.
• Knowledge of common safety hazards and precautions to establish a safe work environment.
• Skill in identifying problems and recommending solutions.
• Skill in preparing and maintaining records, writing reports, and responding to correspondence.
• Skill in developing and maintaining department quality assurance.
• Skill in establishing and maintaining effective working relationships with patients, medical staff, and the public.
• Ability to maintain quality control standards.
• Ability to react calmly and effectively in emergency situations.
• Ability to interpret, adapt, and apply guidelines and procedures.
• Ability to communicate clearly.
• Knowledge of safety requirements and ability to recognize and correct hazardous conditions.